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but-2-enyl(trimethoxy)silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13436-83-4

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13436-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13436-83-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,3 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13436-83:
(7*1)+(6*3)+(5*4)+(4*3)+(3*6)+(2*8)+(1*3)=94
94 % 10 = 4
So 13436-83-4 is a valid CAS Registry Number.

13436-83-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name but-2-enyl(trimethoxy)silane

1.2 Other means of identification

Product number -
Other names Crotyltrimethoxysilane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13436-83-4 SDS

13436-83-4Relevant academic research and scientific papers

BINAP/AgOTf/KF/18-crown-6 as new bifunctional catalysts for asymmetric Sakurai-Hosomi allylation and Mukaiyama aldol reaction

Wadamoto, Manabu,Ozasa, Nobuko,Yanagisawa, Akira,Yamamoto, Hisashi

, p. 5593 - 5601 (2007/10/03)

A catalytic amount of KF·18-crown-6 complex is effective as a soluble fluoride source to activate an asymmetric Sakurai-Hosomi allylation with BINAP and silver(I) triflate catalyst. The allylation of a variety of aromatic, α,β-unsaturated and aliphatic al

Pentacoordinate Allylsiliconates in Organic Synthesis: Synthesis of Triethylammonium Bis(catecholato)allylsiliconates and Selective Allylation of Aldehydes

Hosomi, Akira,Kohra, Shinya,Ogata, Koichiro,Yanagi, Toshiharu,Tominaga, Yoshinori

, p. 2415 - 2420 (2007/10/02)

Pentacoordinate triethylammonium bis(catecholato)allylsiliconates were synthesized by reaction of allyltrialkoxysilanes, catechol, and triethylamine.The allylsiliconates react with aldehydes without catalyst to give the corresponding homoallyl alcohols in high yields in a completely regiospecific and highly diastereoselective mode.The stereochemistry of the products can be reasonably interpreted by assuming a cyclic six-membered ring transition state.This allylation of aldehydes can also be effected by mixing them with an allyltrialkoxysilane, an alcohol, and an amide, generating the allylsiliconate in situ.

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